JP2013534144A5 - - Google Patents

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JP2013534144A5
JP2013534144A5 JP2013524893A JP2013524893A JP2013534144A5 JP 2013534144 A5 JP2013534144 A5 JP 2013534144A5 JP 2013524893 A JP2013524893 A JP 2013524893A JP 2013524893 A JP2013524893 A JP 2013524893A JP 2013534144 A5 JP2013534144 A5 JP 2013534144A5
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composition
temperature
bioorganic
surfactant
host cell
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Priority claimed from PCT/US2011/047616 external-priority patent/WO2012024186A1/en
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図5は、ボルテックスミキサー、回転ミキサー、撹拌子、及びULTRA-TURRAX(登録商標)分散機を含む異なる方法で混合された試料の保持/混合時間に応じた油放出率のプロットである。FIG. 5 is a plot of oil release rate as a function of retention / mixing time for samples mixed in different ways including a vortex mixer , rotary mixer, stir bar, and ULTRA-TURRAX® disperser.

油相の水相に対する比は、組成物又はエマルションのPITに影響を与え得る。一般に、PITは、油相の水相に対する比の上昇と共に上昇する。さらに、界面活性剤の濃度が低ければ低いほど、PITの上昇率が高くなる。一部の実施態様では、油相の水相に対する比は、約1:100〜約100:1、約1:50〜約50:1、約1:20〜約20:1、約1:10〜約10:1、約1:8〜約8:1、約1:6〜約6:1、約1:5〜約5:1、約1:4〜約4:1、約1:3〜約3:1、又は約1:2〜約2:1である。
The ratio of oil phase to water phase can affect the PIT of the composition or emulsion. In general, PIT increases with increasing ratio of oil phase to water phase. Furthermore, the lower the surfactant concentration, the higher the rate of increase in PIT. In some embodiments, the ratio of oil phase to aqueous phase is about 1: 100 to about 100: 1, about 1:50 to about 50: 1 , about 1:20 to about 20: 1, about 1:10. To about 10: 1, about 1: 8 to about 8: 1, about 1: 6 to about 6: 1, about 1: 5 to about 5: 1, about 1: 4 to about 4: 1, about 1: 3 To about 3: 1, or from about 1: 2 to about 2: 1.

別の例では、精製組成物を、キレート剤の添加により仕上げ精製して該組成物中の金属の量を減少させることができる。特定の実施態様では、精製工程は、キレート剤の添加によって粗生物有機組成物中に存在する金属を除去する工程も含む。任意の適切なキレート剤を使用することができる。適切なキレート剤の実例として、アスコルビン酸、クエン酸、マレイン酸、シュウ酸、コハク酸、ジカルボキシメチルルタミン酸、エチレンジアミンジコハク酸(EDDS)、及びエチレンジアミンテトラ酢酸(EDTA)などが挙げられる。
In another example, the purified composition can be final purified by the addition of a chelating agent to reduce the amount of metal in the composition. In certain embodiments, the purification step also includes removing metals present in the crude bioorganic composition by the addition of a chelating agent. Any suitable chelating agent can be used. Illustrative of suitable chelating agents, ascorbic acid, citric acid, maleic acid, oxalic acid, succinic acid, di-carboxymethyl glutamic acid, ethylenediamine disuccinic acid (EDDS), and the like ethylenediaminetetraacetic acid (EDTA).

Claims (15)

(a)界面活性剤、宿主細胞、水性媒体、該宿主細胞によって産生された生物有機化合物、及びそこから形成される水中油型エマルションを含む組成物を提供する工程であって、該水性媒体中の該界面活性剤の溶解度が、温度上昇と共に低下し、該組成物の温度が、該組成物の相反転温度よりも少なくとも約1℃低い、前記工程;
(b)該水中油型エマルションの温度を、該相反転温度よりも少なくとも約1℃高い温度まで上昇させ、それによって、該水中油型エマルションを油中水型エマルションに変換する工程;及び
(c)該組成物の液液分離を行って粗生物有機組成物を提供する工程を含む、方法。
(a) providing a composition comprising a surfactant, a host cell, an aqueous medium, a bio-organic compound produced by the host cell, and an oil-in-water emulsion formed therefrom, comprising the step of: Wherein the solubility of the surfactant decreases with increasing temperature, and the temperature of the composition is at least about 1 ° C. lower than the phase inversion temperature of the composition;
(b) raising the temperature of the oil-in-water emulsion to a temperature at least about 1 ° C. above the phase inversion temperature, thereby converting the oil-in-water emulsion to a water-in-oil emulsion; and
(c) A method comprising liquid-liquid separation of the composition to provide a crude bioorganic composition.
前記組成物が、水中油型エマルションである、請求項1記載の方法。   The method of claim 1, wherein the composition is an oil-in-water emulsion. 前記工程(b)の前に前記組成物の量を減少させる工程であって、前記生物有機化合物の実質的に全てが該組成物中に残留する、前記工程をさらに含む、請求項1又は2記載の方法。   The method further comprising the step of reducing the amount of the composition prior to step (b), wherein substantially all of the bioorganic compound remains in the composition. The method described. 前記組成物の量を、約75%以上減少させる、請求項3記載の方法。   4. The method of claim 3, wherein the amount of the composition is reduced by about 75% or more. 前記工程(a)における前記温度が、前記相反転温度よりも少なくとも約5℃又は少なくとも約10℃低く、前記工程(b)における前記温度が、前記相反転温度よりも少なくとも約5℃又は少なくとも約10℃又は少なくとも約15℃高い温度まで上昇させる、請求項1〜4のいずれか1項記載の方法。   The temperature in step (a) is at least about 5 ° C. or at least about 10 ° C. lower than the phase inversion temperature, and the temperature in step (b) is at least about 5 ° C. or at least about at least about the phase inversion temperature. 5. A method according to any one of claims 1 to 4 wherein the temperature is increased to 10C or at least about 15C higher. 前記粗生物有機組成物を精製して精製生物有機組成物を得る工程をさらに含む、請求項1〜5のいずれか1項記載の方法。   6. The method according to any one of claims 1 to 5, further comprising the step of purifying the crude bioorganic composition to obtain a purified bioorganic composition. 前記粗生物有機組成物の精製が、フラッシュ蒸留によるものである、請求項6記載の方法。   7. The method of claim 6, wherein the purification of the crude bioorganic composition is by flash distillation. 前記精製生物有機組成物を酸化防止剤又はフェノール系酸化防止剤で処理する工程をさらに含む、請求項6記載の方法。   7. The method of claim 6, further comprising treating the purified bioorganic composition with an antioxidant or a phenolic antioxidant. 界面活性剤、宿主細胞、水性媒体、及び該宿主細胞によって産生された生物有機化合物を含む組成物であって、該水性媒体中の該界面活性剤の溶解度が、温度上昇と共に低下し、該組成物の温度が、該組成物の相反転温度よりも少なくとも約1℃高く、該生物有機化合物が、イソプレノイドである、前記組成物。   A composition comprising a surfactant, a host cell, an aqueous medium, and a bioorganic compound produced by the host cell, wherein the solubility of the surfactant in the aqueous medium decreases with increasing temperature, and the composition The composition wherein the temperature of the product is at least about 1 ° C. higher than the phase inversion temperature of the composition and the bioorganic compound is an isoprenoid. 前記界面活性剤が非イオン性界面活性剤を含むか、又は前記界面活性剤がポリエーテルポリオール、ポリオキシエチレンC8-20-アルキルエーテル、ポリオキシエチレンC8-20-アルキルアリールエーテル、ポリオキシエチレンC8-20-アルキルアミン、ポリオキシエチレンC8-20-アルケニルエーテル、ポリオキシエチレンC8-20-アルケニルアミン、ポリエチレングリコールアルキルエーテル、又はこれらの組み合わせ;或いはポリエーテルポリオール、ポリオキシエチレンノニルフェニルエーテル、ポリオキシエチレンドデシルフェニルエーテル、又はこれらの組み合わせを含む、請求項9記載の組成物又は請求項1〜8のいずれか1項記載の方法。 The surfactant comprises a nonionic surfactant, or the surfactant is a polyether polyol, polyoxyethylene C 8-20 -alkyl ether, polyoxyethylene C 8-20 -alkyl aryl ether, polyoxy Ethylene C 8-20 -alkylamine, polyoxyethylene C 8-20 -alkenyl ether, polyoxyethylene C 8-20 -alkenylamine, polyethylene glycol alkyl ether, or combinations thereof; or polyether polyol, polyoxyethylene nonyl 9. The composition of claim 9 or the method of any one of claims 1-8, comprising phenyl ether, polyoxyethylene dodecyl phenyl ether, or a combination thereof. 前記組成物の温度が、前記相反転温度よりも少なくとも約5℃、少なくとも約10℃、又は少なくとも約15℃高い、請求項9〜10のいずれか1項記載の組成物。   11. The composition of any one of claims 9 to 10, wherein the temperature of the composition is at least about 5 ° C, at least about 10 ° C, or at least about 15 ° C higher than the phase inversion temperature. 前記生物有機化合物が、炭化水素、又はイソプレノイド、又はファルネセンであり、かつ該ファルネセンが、α-ファルネセン、β-ファルネセン、又はこれらの組み合わせである、請求項9〜10のいずれか1項記載の組成物又は請求項1〜8のいずれか1項記載の方法。   The composition according to any one of claims 9 to 10, wherein the bioorganic compound is a hydrocarbon, isoprenoid, or farnesene, and the farnesene is α-farnesene, β-farnesene, or a combination thereof. Or a process according to any one of claims 1-8. 前記宿主細胞が、細菌、真菌、藻、又はこれらの組み合わせである、請求項9〜12のいずれか1項記載の組成物又は請求項1〜8のいずれか1項記載の方法。   The composition according to any one of claims 9 to 12, or the method according to any one of claims 1 to 8, wherein the host cell is a bacterium, a fungus, an algae, or a combination thereof. 前記宿主細胞が、エシェリキア属、バシラス属、ラクトバシラス属、クリベロミセス属、ピチア属、サッカロミセス属、ヤロウイア属、サッカロミセス・セレビシエ、クロレラ・ミヌティッシマ、クロレラ・エマゾーニ、クロレラ・ソロキニアナ、クロレラ・エリプソイデア、クロレラ属の種、クロレラ・プロトセコイデス、及びこれらの組み合わせから選択される、請求項9〜12のいずれか1項記載の組成物又は請求項1〜8のいずれか1項記載の方法。   The host cell is Escherichia, Bacillus, Lactobacillus, Criveromyces, Pichia, Saccharomyces, Yarrowia, Saccharomyces cerevisiae, Chlorella Minutissima, Chlorella emazoni, Chlorella solokiniana, Chlorella ellipsoida, 13. A composition according to any one of claims 9-12 or a method according to any one of claims 1-8, selected from species, Chlorella protosequoides, and combinations thereof. 前記組成物がエマルションである、請求項9〜14のいずれか1項記載の組成物。   15. The composition according to any one of claims 9 to 14, wherein the composition is an emulsion.
JP2013524893A 2010-08-16 2011-08-12 Method for purifying bioorganic compounds from fermentation broths containing surfactants by temperature-induced phase inversion Pending JP2013534144A (en)

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US37387610P 2010-08-16 2010-08-16
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